Searched for: school:SOM
Department/Unit:Population Health
Diabetes, GDF-15 and incident heart failure: the atherosclerosis risk in communities study
Echouffo-Tcheugui, Justin B; Daya, Natalie; Ndumele, Chiadi E; Matsushita, Kunihiro; Hoogeveen, Ron C; Ballantyne, Christie M; Coresh, Josef; Shah, Amil M; Selvin, Elizabeth
AIMS/HYPOTHESIS:Elevated circulating growth differentiation factor-15 (GDF-15), a marker of cellular stress, is associated with both heart failure (HF) and diabetes. However, it is unclear to what extent GDF-15 is associated with HF among individuals with and without diabetes. METHODS:We evaluated 10,570 participants free of HF at Visit 3 (1993-1995) of the Atherosclerosis Risk in Communities study. We used Cox regression to evaluate the joint associations of GDF-15 and diabetes with incident HF. Models were adjusted for traditional cardiovascular risk factors. RESULTS:Among a total of 10,570 individuals (mean age of 60.0 years, 54% women, 27% black adults), elevated GDF-15 (≥75th percentile) was more common in people with diabetes compared with those without diabetes (32.8% vs 23.6%, p<0.0001). During 23 years of follow-up, there were 2429 incident HF events. GDF-15 (in quartiles) was independently associated with HF among those with and without diabetes, with a stronger association among individuals with diabetes (p-for-diabetes-GDF-15 interaction = 0.034): HR for highest vs lowest GDF-15 quartile (reference): 1.64 (95% CI 1.41, 1.91) among those without diabetes and 1.72 (95% CI 1.32, 2.23) among those with diabetes. Individuals with diabetes and elevated GDF-15 had the highest risk of incident HF (HR 2.46; 95% CI 1.99, 3.03). After accounting for HF risk factors, GDF-15 provided additional prognostic information among participants with diabetes (ΔC statistic for model with vs model without GDF-15: +0.008, p = 0.001) and among those without diabetes (+0.006, p<0.0001). CONCLUSIONS/INTERPRETATION:In a community-based sample of US adults, GDF-15 provided complementary prognostic information on the HF risk, especially among individuals with diabetes.
PMCID:9081127
PMID: 35275240
ISSN: 1432-0428
CID: 5586512
Increasing Motivation for Lifestyle Change Is Not Enough to Treat Obesity
Wittleder, Sandra; Jay, Melanie
PMID: 35344377
ISSN: 1539-3704
CID: 5219822
Apparent lack of association of COVID-19 vaccination with Herpes Zoster
Patil, Sachi A; Dygert, Levi; Galetta, Steven L; Balcer, Laura J; Cohen, Elisabeth J
Purpose/UNASSIGNED:Herpes zoster (HZ) has been identified as a potential association with the BNT162b2 COVID-19 vaccination. This study evaluated this possible association in a cohort of patients receiving the vaccination. Methods/UNASSIGNED:Epic electronic health records of adult patients who received at least one COVID-19 vaccination between January 12, 2020 and 9/30/2021 within the NYU Langone Health were reviewed to analyze a new diagnosis of herpes zoster within 3 months before compared to 3 months after vaccination. Results/UNASSIGNED:Of the 596,111 patients who received at least one COVID-19 vaccination, 716 patients were diagnosed with HZ within three months prior to vaccination, compared to 781 patients diagnosed within 3 months afterwards. Using the chi-square test for independence of proportions, there was not a statistically significant difference in frequency of HZ before (proportion: 0.0012, 95% CI: [0.0011, 0.0013]) vs. after vaccination (proportion: 0.0013, 95% CI: [0.0012, 0.0014]); (p = 0.093). Conclusions and importance/UNASSIGNED:This study did not find evidence of an association between COVID-19 vaccination and a new diagnosis of HZ. We encourage health care professionals to strongly recommend COVID-19 vaccinations per Centers for Disease Control (CDC) recommendations and vaccination against HZ according to Food and Drug Administration (FDA) approval for the recombinant zoster vaccine.
PMCID:9021123
PMID: 35474754
ISSN: 2451-9936
CID: 5217432
Electronic health record data may lead to underestimates of cannabis use-Especially among older populations [Editorial]
Palamar, Joseph J; Le, Austin
PMID: 35234290
ISSN: 1532-5415
CID: 5174432
The Prenatal Neighborhood Environment and Geographic Hotspots of Infants with At-risk Birthweights in New York City
Duh-Leong, Carol; Shonna Yin, H; Gross, Rachel S; Elbel, Brian; Thorpe, Lorna E; Trasande, Leonardo; White, Michelle J; Perrin, Eliana M; Fierman, Arthur H; Lee, David C
Infants born with low or high ("at-risk") birthweights are at greater risk of adverse health outcomes across the life course. Our objective was to examine whether geographic hotspots of low and high birthweight prevalence in New York City had different patterns of neighborhood risk factors. We performed census tract-level geospatial clustering analyses using (1) birthweight prevalence and maternal residential address from an all-payer claims database and (2) domains of neighborhood risk factors (socioeconomic and food environment) from national and local datasets. We then used logistic regression analysis to identify specific neighborhood risk factors associated with low and high birthweight hotspots. This study examined 2088 census tracts representing 419,025 infants. We found almost no overlap (1.5%) between low and high birthweight hotspots. The majority of low birthweight hotspots (87.2%) overlapped with a socioeconomic risk factor and 95.7% overlapped with a food environment risk factor. Half of high birthweight hotspots (50.0%) overlapped with a socioeconomic risk factor and 48.8% overlapped with a food environment risk factor. Low birthweight hotspots were associated with high prevalence of excessive housing cost, unemployment, and poor food environment. High birthweight hotspots were associated with high prevalence of uninsured persons and convenience stores. Programs and policies that aim to prevent disparities in infant birthweight should examine the broader context by which hotspots of at-risk birthweight overlap with neighborhood risk factors. Multi-level strategies that include the neighborhood context are needed to address prenatal pathways leading to low and high birthweight outcomes.
PMID: 35641714
ISSN: 1468-2869
CID: 5233372
Addressing breast cancer surgical disparities using a community-clinical linkage patient navigation model strategy in a NYC hospital system [Editorial]
Joseph, Kathie-Ann
PMID: 35115173
ISSN: 1879-1883
CID: 5153842
Climate cardiology
Hadley, Michael B; Vedanthan, Rajesh; Ebi, Kristie L; Fuster, Valentin
PMCID:9185672
PMID: 35654448
ISSN: 2059-7908
CID: 5277652
Remission of T2DM requires early diagnosis and substantial weight reduction
Bergman, Michael; Buysschaert, Martin; Medina, José Luiz; Tuomilehto, Jaakko
PMID: 35393576
ISSN: 1759-5037
CID: 5219702
Changes in Serum Intact Fibroblast Growth Factor 23 Concentrations From Midlife to Late Life and Their Predictors in the Community: The ARIC Study
Ishigami, Junichi; Honda, Yasuyuki; Karger, Amy B; Coresh, Josef; Selvin, Elizabeth; Lutsey, Pamela L; Matsushita, Kunihiro
OBJECTIVE/UNASSIGNED:To investigate longitudinal changes in the blood concentration of fibroblast growth factor 23 (FGF23) from midlife to late life and their major predictors in the general population. PATIENTS AND METHODS/UNASSIGNED:In 14,444 participants of the Atherosclerosis Risk in Communities Study, we analyzed the association of 31,095 measurements of serum intact FGF23 with age using data from 3 visits (visit 2 [N=13,460; mean age, 57 years]; visit 3 [N=12,323; mean age, 60 years]; and visit 5 [N=6122; mean age, 76 years]) and a linear mixed-effects model. Among 5804 participants who had FGF23 measurements at both visits 3 and 5, we explored predictors of FGF23 change from midlife to late life using linear regression models. Prespecified risk factors were estimated glomerular filtration rate, body mass index, ever smoking, ever drinker, diabetes, hypertension, history of cardiovascular disease, total cholesterol, and high-density lipoprotein cholesterol. RESULTS/UNASSIGNED:(ΔFGF23, +4.4 pg/mL [95% CI, 0.9 to 8.0]), diabetes vs no diabetes (ΔFGF23, +6.2 pg/mL [95% CI, 4.1 to 8.3]), and hypertension vs no hypertension (ΔFGF23, +4.1 pg/mL [95% CI, 2.7 to 5.4]). CONCLUSION/UNASSIGNED:FGF23 did not show any major changes in midlife but increased linearly in late life. Reduced kidney function, diabetes, and hypertension were robustly associated with a greater increase in FGF23. Further investigations are needed to understand the potential mechanisms linking these conditions to an increase in FGF23 concentrations.
PMCID:9062741
PMID: 35517245
ISSN: 2542-4548
CID: 5586582
Injecting Opioid Use Disorder Treatment in Jails and Prisons: The Potential of Extended-release Buprenorphine in the Carceral Setting
Berk, Justin; Del Pozo, Brandon; Rich, Josiah D; Lee, Joshua D
As the opioid overdose cases rise, policy-makers and researchers should target interventions to populations at highest risk. Incarceration serves as a risk factor for opioid overdose (Gan et al. Addiction 2021) and a large portion of recent overdose deaths have had encounters in the criminal justice system. Medications for opioid use disorder in the criminal justice system can save lives, though unique administrative barriers in jails and prisons hinder access. As facilities expand medications for opioid use disorder access (due to new legislation and court rulings across states), extended-release buprenorphine offers an opportunity to overcome these barriers including logistics of administration, diversion concern, patient stigma, and an increased bridge of treatment during re-entry to the community. As extended-release buprenorphine has practical advantages in correctional health delivery, future research and policy discussions should investigate its optimal role in treating opiate addiction in a carceral setting.
PMID: 34954747
ISSN: 1935-3227
CID: 5107942